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Description
Working individually or in a team environment identifies and and puts into place corrective actions to address potential or actual process failures(equipment, procedural, people or materials). The key role of the position is to ensure that throughout a product's lifecycle (development through commericalization) quality is designed into products by understanding and controlling the processes used to manufacture and test the product. Assumes responsibility for the development of metrics that report on the effectiveness of processes, status of improvement opportunities and progress against performance objectives. Key interactions and interfaces are with Production Management, Project Team Leaders and team members, QA/QC, Pharmaceutical Technology Operations, Purchasing and material/component/equipment suppliers. Serves as a mentor to staff members on the use of quality tools and measures.
Requires 5 years experience as a Quality Engineer in a cGMP environment and leadership skills to enable them to take the lead. Prefer experience in pharmaceutical tablet manufacturing or tablet development. KT problem solving certification,Lean Manufacturing/Six Sigma Training, Supplier Certification. Advanced degree in Engineering, Science or Math
Please submit resumes via Visium Resources website:
www.myvisium.com
Call Robert Denmon 800-913-0903 for more details
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